The United States Department of Agriculture (USDA) recently proposed a Bioengineered Food Disclosure rule, which provides food companies with guidance on ways to label products made with genetically modified ingredients and identifies which products are covered. This important USDA proposal implements the National Bioengineered Food Disclosure Law of 2016 – and will impact most food companies and their products. Do you understand the key requirements of the proposed rule – and how it will impact you?
Join this session with regulatory consultant, Norma Skolnik, who will help you understand the key requirements of the National Bioengineered Food Disclosure Proposed Rule – such as the ingredients subject to disclosure, the acceptable labeling methods, GMO labeling symbols, thresholds and exemptions, timelines and more.
Skolnik will provide citations to all relevant USDA and FDA laws and regulations, as well as relevant website references and comment submission information, and the know-how tips on how to implement this important new proposed regulation.
Through this information-packed session, you will learn about:
Who Should Attend
Ask a question at the Q&A session following the live event and get advice unique to your situation, directly from our expert speaker.
Norma Skolnik has over 35 years of regulatory experience working with the pharmaceutical and dietary supplement industries. She served as Director of Regulatory Affairs for the Americas for Cadbury Adams. Prior to that, she was Director of Regulatory Affairs for the Adams Division of Pfizer and Associate Director of Regulatory Affairs for the Warner-Lambert company. She also served as Director of Regulatory Affairs for Lederle Consumer Healthcare and...
More Events By The Speaker